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Volumn 49, Issue 1, 2008, Pages 117-121

Sterically encumbered hexakis(alkylseleno)benzenes: conformational behavior of hexakis(iso-propylselenomethyl)benzene toward Hg2+ ions on selective recognition

Author keywords

Hexakis(alkylseleno)benzenes; Hg2+ ions; Ion selective electrodes (ISEs); Molecular recognition

Indexed keywords

1 METHYLNAPHTHALENE; BENZENE DERIVATIVE; HEXAKIS(BROMOMETHYL)BENZENE; HEXAKIS(ISOPROPYLSELENOMETHYL)BENZENE; IONOPHORE; MERCURY; UNCLASSIFIED DRUG;

EID: 36749040307     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2007.11.007     Document Type: Article
Times cited : (17)

References (91)
  • 1
    • 0000692656 scopus 로고    scopus 로고
    • For general discussions concerning inclusion host design based on hexa-hosts of oxygen and sulfur, see:. MacNicol D.D., Toda F., and Bishop R. (Eds), Elsevier Science, Oxford
    • For general discussions concerning inclusion host design based on hexa-hosts of oxygen and sulfur, see:. MacNicol D.D., and Downing G.A. In: MacNicol D.D., Toda F., and Bishop R. (Eds). Comprehensive Supramolecular Chemistry Vol. 6 (1996), Elsevier Science, Oxford 421
    • (1996) Comprehensive Supramolecular Chemistry , vol.6 , pp. 421
    • MacNicol, D.D.1    Downing, G.A.2
  • 2
    • 0003231666 scopus 로고    scopus 로고
    • MacNicol D.D., Toda F., and Bishop R. (Eds), Elsevier Science, Oxford
    • Weber E. In: MacNicol D.D., Toda F., and Bishop R. (Eds). Comprehensive Supramolecular Chemistry Vol. 6 (1996), Elsevier Science, Oxford 535
    • (1996) Comprehensive Supramolecular Chemistry , vol.6 , pp. 535
    • Weber, E.1
  • 4
    • 0000741239 scopus 로고
    • Atwood J.L., Davies J.E.D., and MacNicol D.D. (Eds), Oxford University Press, Oxford
    • Toda F. In: Atwood J.L., Davies J.E.D., and MacNicol D.D. (Eds). Inclusion Compounds Vol. 4 (1991), Oxford University Press, Oxford 126
    • (1991) Inclusion Compounds , vol.4 , pp. 126
    • Toda, F.1
  • 61
    • 0001476014 scopus 로고
    • For similar conformational behavior arising from other hexaheteroatom-substituted benezenes, see:
    • For similar conformational behavior arising from other hexaheteroatom-substituted benezenes, see:. Marsau P. Acta Crystallogr. 18 (1965) 851-854
    • (1965) Acta Crystallogr. , vol.18 , pp. 851-854
    • Marsau, P.1
  • 70
    • 0037125526 scopus 로고    scopus 로고
    • Conformationally hexasubstituted benzenes can also exist in solution in a variety of interconverting conformers from the most stable conformers ababab (a = above, b = below) to the least stable conformer such as aaabab, aaaaab, aaaaaa or bbbbbb.
    • Conformationally hexasubstituted benzenes can also exist in solution in a variety of interconverting conformers from the most stable conformers ababab (a = above, b = below) to the least stable conformer such as aaabab, aaaaab, aaaaaa or bbbbbb. Fukin G.K., Lindeman S.V., and Kochi J.K. J. Am. Chem. Soc. 124 (2002) 8329-8336
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 8329-8336
    • Fukin, G.K.1    Lindeman, S.V.2    Kochi, J.K.3
  • 76
    • 36749099612 scopus 로고    scopus 로고
    • note
    • Crystallographic data for compounds 2, 10 and 11 have been deposited at the Cambridge Crystallographic Data Centre, CCDC Nos. 602913, 602915, and 602914, respectively. Copies of this information may be obtained free of charge from The Director, CCDC, 12 Union Road, Cambridge, CB2 1EZ, UK (+44-1223-336408; e-mail: deposit@ccdc.cam.ac.uk or http://www.ccdc.cam.ac.uk).
  • 80
    • 0032099044 scopus 로고    scopus 로고
    • + present in the solution as observed during the analytical measurements:
    • + present in the solution as observed during the analytical measurements:. Bühlmann P., Pretsch E., and Bakker E. Chem. Rev. 98 (1998) 1593-1688
    • (1998) Chem. Rev. , vol.98 , pp. 1593-1688
    • Bühlmann, P.1    Pretsch, E.2    Bakker, E.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.